http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-108875-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a73cee5001ad08339ae751c10d9abf71 |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B2200-13 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D519-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-28 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-53 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-28 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-437 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4985 |
| filingDate | 2017-06-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8206bfa7bbf28282b6449117720ae278 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_93f836b99512f2719ae3e9542c22df85 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ee39ef63aa1f128526a368379b1e2d56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2c64e71517528f11f95e75f11cbe69b1 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a70736f56690f1c7f35937eff3d6a1c8 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_22ea176ddfed074feb2172976d7a4024 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9a76e8bc72a90ebbf0e7e005360bcbfe http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_05a85e76b052ec29d37af7d02fd6a97b |
| publicationDate | 2018-10-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-108875-A1 |
| titleOfInvention | HETEROCYCLIC COMPOUNDS AS PI3K-g INHIBITORS |
| abstract | These compounds of PI3K-g and which are useful for the treatment of disorders, such as autoimmune diseases, cancer, cardiovascular diseases and neurodegenerative diseases. Claim 1: A compound of the formula (1), or a pharmaceutically acceptable salt or tautomer thereof; where: X¹ is N or CR¹; X² is N or CR²; X³ is N or CR³; X⁴ is N or CR⁴; X⁵ is N or CR⁵; X⁶ is N or CR⁶; X³, X⁴, X⁵ and X⁶ are not simultaneously N; R⁷ is H or C₁₋₆ alkyl optionally substituted with 1, 2 or 3 groups independently selected from halo, OH, oxo, CN, C₃₋₆ cycloalkyl, 4-6 membered heterocycloalkyl, C₆₋₁₀ aryl, C₁₋₆ haloalkyl, C₁₋₆ alkoxy, C₁₋₆ haloalkoxy, NH₂, C₁₋₆-NH- alkyl and (C₁₋₆ alkyl) ₂N-; each of R¹, R², R³, R⁴, R⁵, R⁶ and R⁸ is independently selected H, D, halo, oxo, C₁₋₆ alkoxy, C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₁₋ haloalkyl ₆, C₁₋₆ haloalkoxy, C₆₋₁₀ aryl, C₃₋₁₀ cycloalkyl, 5-10 membered heteroaryl, 4-14 membered heterocycloalkyl, C₆₋₁₀-C₁₋₄-aryl alkyl, C₃₋₁₀-C₁₋ alkyl cycloalkyl ₄-, (5-14 membered heteroaryl) -C₁₋₄ alkyl-, (4-14 membered heterocycloalkyl) -C₁₋₄ alkyl, CN, NO₂, ORᵃ¹, SRᵃ¹, NHORᵃ¹, C (O) Rᵃ¹, C (O) NRᵃ¹Rᵃ¹, C (O) ORᵃ¹, OC (O) Rᵃ¹, OC (O) NRᵃ¹Rᵃ¹, NHRᵃ¹, NRᵃ¹Rᵃ¹, NRᵃ¹C (O) Rᵃ¹, NRᵃ¹C (O) ORᵃ¹, NRᵃ¹C (O) NRᵃ¹Rᵃ¹, C (= NRᵃ¹) Rᵃ¹, C (= NRᵃ¹) NRᵃ¹Rᵃ¹, NRᵃ¹C (= NRᵃ¹) NRᵃ¹Rᵃ¹, NRᵃ¹C (= NOH) NRᵃ¹Rᵃ¹, NRᵃ¹C (= NCN) NRᵃ¹Rᵃ¹, NRᵃ¹S (O) Rᵃ¹, NRᵃ¹S (O) ₂Rᵃ¹, NRᵃ¹S (O) ₂NRᵃ¹Rᵃ¹, S ( O) Rᵃ¹, S (O) NRᵃ¹Rᵃ¹, S (O) ₂Rᵃ¹, SF₅, -P (O) Rᵃ¹Rᵃ¹, -P (O) (ORᵃ¹) (ORᵃ¹), B (ORᵃ¹) ₂ and S (O) ₂NRᵃ¹Rᵃ¹, where each of the C₁₋₆ alkyl, C₁₋ alkoxy ₆, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₆₋₁₀ aryl, C₃₋₁₀ cycloalkyl, 5-10 heteroaryl, 4-14 membered heterocycloalkyl, C₆₋₁₀ aryl-C₁₋₄- alkyl, C₃₋₁₀ cycloalkyl -C₁₋₄ alkyl, (5-14 membered heteroaryl) -C₁₋₄ alkyl- and (4-14 membered heterocycloalkyl) -C₁₋₄ alkyl of R¹, R², R³, R⁴, R⁵, R⁶ and R⁸ it is optionally substituted with 1, 2, 3, 4 or 5 independently selected Rᵇ substituents; R⁹ is H, D, CN, C (O), NH₂, -OH, -COOH, -NH (C₁₋₆ alkyl), -NH (C₁₋₆ alkyl) ₂, C₁₋₆ alkyl, C₁₋₆ haloalkyl, C₁₋₆ alkoxy or C₁₋₆ haloalkoxy, where the C₁₋₆ alkyl is optionally substituted with 1, 2 or 3 independently selected Rq substituents; R¹⁰ is selected from H, C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₁₋₆ haloalkyl, C₁₋₆ alkoxy, C₁₋₆ haloalkoxy, C₆₋₁₀ aryl, C₃₋₁₀ cycloalkyl, 5 - heteroaryl 10 members, 4-14 membered heterocycloalkyl, C₆₋₁₀-C₁₋₄- alkyl, C₃₋₁₀-C₁₋₄- cycloalkyl, (5-14 membered heteroaryl) -C₁₋₄- alkyl, (heterocycloalkyl of 4 - 14 members) - C₁₋₄-, ORᵃ², SRᵃ², NHORᵃ², C (O) Rᵃ², C (O) NRᵃ²Rᵃ², C (O) ORᵃ², NHRᵃ², NRᵃ²Rᵃ², NRᵃ²C (O) Rᵃ², NRᵃ²C (O) ORᵃ², NRᵃ²C (O) NRᵃ²Rᵃ², C (= NRᵃ²) Rᵃ², C (= NRᵃ²) NRᵃ²Rᵃ², NRᵃ²C (= NRᵃ²) NRᵃ²Rᵃ², NRᵃ²S (O) Rᵃ², NRᵃ²S (O) ₂Rᵃ², NRᵃ²S (O) ₂NRᵃ²R (R) ) Rᵃ², S (O) NRᵃ²Rᵃ², S (O) ₂Rᵃ² and S (O) ₂NRᵃ²Rᵃ², where each of the C₁₋₆ alkyl, C₁₋₆ alkoxy, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₆₋₁₀ aryl, cycloalkyl C ₋₁₀, 5-14 membered heteroaryl, 4-10 membered heterocycloalkyl, C₆₋₁₀-C₁₋₄-alkyl, C₃₋₁₀-C ciclo-cycloalkyl, (5-14 membered heteroaryl) -C₁ alkyl ₋₄ and (4-14 membered heterocycloalkyl) -C₁₋₄ -alkyl of R¹⁰ is optionally substituted with 1, 2, 3, 4, 5, 6, 7 or 8 independently selected Rᵇ substituents; L is a moiety of formula (2), of formula (3) or -SO₂-, where each R¹¹ is independently H, C alquilo alkyl or C₃₋₁₀ cycloalkyl, optionally substituted with 1 or 2 Rq substituents and where the wavy line single indicates the coupling point with R¹⁰ and the double wavy line indicates the coupling point with the 6-member ring A; or when L is the remainder of formula (2), R¹⁰ and R¹¹ taken together optionally with the nitrogen atom to which they are attached form a heterocycloalkyl of 4 to 14 heterocycloalkyl members or 4 to 14 alkyl C₁₋₄ members having 0 to 14 additional heteroatoms as ring members, each of which is independently selected from N, O and S, where the 4- to 14-membered heterocycloalkyl consisting of R¹⁰, R¹¹ and N is optionally substituted with 1, 2, 3, 4 , 5 6, 7 or 8 independently selected Rᵇ substituents; each Rᵃ¹ and Rᵃ² is independently selected from H, C₁₋₆ alkyl, C₁₋₄ haloalkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₆₋₁₀ aryl, C₃₋₁₀ cycloalkyl, 5-10 membered heteroaryl, 4-heterocycloalkyl - 14 members, C₆₋₁₀-aryl-C alquilo-alkyl, C₃₋₁₀-cycloalkyl-C₁₋₄-alkyl, (5-10-membered heteroaryl) -C₁₋₄ -alkyl and (4-14-membered heterocycloalkyl) - C₁₋₄- alkyl, where each of the C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₆₋₁₀ aryl, C₃₋₁₀ cycloalkyl, 5-10 membered heteroaryl, 4-14 membered heterocycloalkyl, aryl C₆₋₁₀-C₁₋₄-C alquilo-C₃₋₁₀-C₁₋₄-alkyl-alkyl, (5-10 membered heteroaryl) -C₁₋₄-alkyl and (4-14-membered heterocycloalkyl) -C₁₋₄-alkyl Rᵃ¹ and Rᵃ² is optionally substituted with 1, 2, 3, 4 or 5 independently selected Rᵈ substituents; each Rᵇ substituent is independently selected from D, halo, oxo, C₁₋₄ alkyl, C₁₋₆ alkoxy, C₁₋₄ haloalkyl, C₁₋₄ haloalkoxy, C₆₋₁₀ aryl, C₃₋₁₀ cycloalkyl, 5-10 membered heteroaryl, 4-14 membered heterocycloalkyl, C₆₋₁₀-C₁₋₄- alkyl, C₃₋₁₀-C ciclo- cycloalkyl, (5-10 membered heteroaryl) -C₁₋₄ alkyl (4-14 membered heterocycloalkyl) -alkyl C₁₋₄-, CN, OH, NH₂, NO₂, NHORᶜ, ORᶜ, SRᶜ, C (O) Rᶜ, C (O) NRᶜRᶜ, C (O) ORᶜ, OC (O) Rᶜ, OC (O) NRᶜRᶜ , C (= NRᶜ) NRᶜRᶜ, NRᶜC (= NRᶜ) NRᶜRᶜ, NRᶜC (= NOH) NRᶜRᶜ, NRᶜC (= NCN) NRᶜRᶜ, SF₅, -P (O) RᶜRᶜ, -P (O) (ORᶜ) (ORᶜ), NHRᶜ, NRᶜRᶜ, NRᶜC (O) Rᶜ, NRᶜC (O) ORᶜ, NRᶜC (O) NRᶜRᶜ, NRᶜS (O) Rᶜ, NRᶜS (O) ₂Rᶜ, NRᶜS (O) ₂NRᶜRᶜ, S (O) Rᶜ, S (O) NRᶜRᶜ, S (O) ₂Rᶜ or S (O) ₂NRᶜRᶜ; where each of the C₁₋₄ alkyl, C₁₋₆ alkoxy C₁₋₄ haloalkyl, C₁₋₄ haloalkoxy, C₆₋₁₀ aryl, C₃₋₁₀ cycloalkyl, 5-10 membered heteroaryl, 4-14 membered heterocycloalkyl, C₆₋ aryl ₁₀-C₁₋₄-alkyl, C₃₋₁₀-cycloalkyl-C₁₋₄-alkyl, (5-10 membered heteroaryl) -C₁₋₄-alkyl and (4-14-membered heterocycloalkyl) -C₁₋₄- alkyl of Rᵇ it is optionally further substituted with 1, 2 or 3 independently selected Rᵈ substituents; each Rᶜ is independently selected from H, D, C₁₋₆ alkyl, C₁₋₄ haloalkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₆₋₁₀ aryl, C₃₋₁₀ cycloalkyl, 5-10 membered heteroaryl, 4-heterocycloalkyl - 10 members, C₆₋₁₀-aryl-C alquilo-alkyl, C₃₋₁₀-cycloalkyl-C₁₋₄-alkyl, (5-10-membered heteroaryl) -C₁₋₄ -alkyl and (4-10-membered heterocycloalkyl) - C₁₋₄- alkyl, where each of the C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₆₋₁₀ aryl, C₃₋₁₀ cycloalkyl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, aryl C₆₋₁₀-C₁₋₄-alkyl, C₃₋₁₀-cycloalkyl-C₁₋₄-alkyl, (5-10 membered heteroaryl) -C₁₋₄-alkyl and (4-10-membered heterocycloalkyl) -C₁₋₄-alkyl of Rᶜ is optionally substituted with 1, 2, 3, 4 or 5 independently selected Rᵈ substituents; each Rᶠ is independently selected from C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₆₋₁₀ aryl, C₃₋₁₀ cycloalkyl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, C₆₋₁₀-aryl-C alquilo-alkyl, C₃₋₁₀-cycloalkyl-C₁₋₄-alkyl, (5-10 membered heteroaryl) -C₁₋₄-alkyl and (4-10-membered heterocycloalkyl) -C₁₋₄ alkyl -, halo, CN, NHORᵍ, ORᵍ, SRᵍ, C (O) Rᵍ, C (O) NRᵍRᵍ, C (O) ORᵍ, OC (O) Rᵍ, OC (O) NRᵍRᵍ, NHRᵍ, NRᵍRᵍ, NRᵍC (O) Rᵍ, NRᵍC (O) NRᵍRᵍ, NRᵍC (O) ORᵍ, C (= NRᵍ) NRᵍRᵍ, NRᵍC (= NRᵍ) NRᵍRᵍ, NRᵍC (= NOH) NRᵍRᵍ, NRᵍC (= NCN) NRᵍRᵍ, SF₅, -P (O) RᵍRᵍ , -P (O) (ORᵍ) (ORᵍ), S (O) Rᵍ, S (O) NRᵍRᵍ, S (O) ₂Rᵍ, NRᵍS (O) ₂Rᵍ, NRᵍS (O) ₂NRᵍRᵍ and S (O) ₂NRᵍRᵍ; where each of the C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl C₆₋₁₀ aryl, C₃₋₁₀ cycloalkyl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, C₆₋ aryl ₁₀-C₁₋₄-alkyl, C₃₋₁₀-cycloalkyl-C₁₋₄-alkyl, (5-10 membered heteroaryl) -C₁₋₄-alkyl and (4-10-membered heterocycloalkyl) -C₁₋₄- alkyl of Rᶠ it is optionally substituted by 1, 2, 3, 4 or 5 independently selected Rⁿ substituents; each Rⁿ is independently selected from C₁₋₄ alkyl, C₁₋₄ haloalkyl, halo, CN, Rᵒ, NHORᵒ, ORᵒ, SRᵒ, C (O) Rᵒ, C (O) NRᵒRᵒ, C (O) ORᵒ, OC (O) Rᵒ, OC (O) NRᵒRᵒ, NHRᵒ, NRᵒRᵒ, NRᵒC (O) Rᵒ, NRᵒC (O) NRᵒRᵒ, NRᵒC (O) ORᵒ, C (= NRᵒ) NRᵒRᵒ, NRᵒC (= NRᵒ) NRᵒRᵒ, NRᵒC (= NOH) NRᵒRᵒ , NRᵒC (= NCN) NRᵒRᵒ, SF₅, -P (O) RᵒRᵒ, P (O) (ORᵒ) (ORᵒ), S (O) Rᵒ, S (O) NRᵒRᵒ, S (O) ₂Rᵒ, NRᵒS (O) ₂Rᵒ, NRᵒS (O) ₂NRᵒRᵒ and S (O) ₂NRᵒRᵒ; each Rᵈ is independently selected from D, oxo, C₁₋₆ alkyl, C₁₋₆ haloalkyl, halo, C₃₋₁₀ cycloalkyl, C₆₋₁₀ aryl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, C₆₋₁₀ aryl -C₁₋₄ alkyl C₃₋₁₀-C₁₋₄ alkyl-, (5-10 membered heteroaryl) -C₁₋₄ alkyl- and (4-10 membered heterocycloalkyl) -C₁₋₄ alkyl, CN, NH₂, NHORᵉ, ORᵉ, SRᵉ, C (O) Rᵉ, C (O) NRᵉRᵉ, C (O) ORᵉ, OC (O) Rᵉ, OC (O) NRᵉRᵉ, NHRᵉ, NRᵉRᵉ, NRᵉC (O) Rᵉ, NRᵉC (O) NRᵉRᵉ, NRᵉC (O) ORᵉ, C (= NRᵉ) NRᵉRᵉ, NRᵉC (= NRᵉ) NRᵉRᵉ, NRᵉC (= NOH) NRᵉRᵉ, NRᵉC (= NCN) NRᵉRᵉ, SF₅, -P (O) RᵉRᵉ, -P (O) (ORᵉ) (ORᵉ), S (O) Rᵉ, S (O) NRᵉRᵉ, S (O) ₂Rᵉ, NRᵉS (O) ₂Rᵉ, NRᵉS (O) ₂NRᵉRᵉ and S (O) ₂NRᵉRᵉ, where each of the C₁₋ alkyl ₆, C₃₋₁₀ cycloalkyl, C₆₋₁₀ aryl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, C₆₋ aryl ₀-C₁₋₄-alkyl, C₃₋₁₀-cycloalkyl-C₁₋₄-alkyl, (5-10 membered heteroaryl) -C₁₋₄-alkyl and (4-10-membered heterocycloalkyl) -C₁₋₄- alkyl of Rᵈ it is optionally substituted with 1, 2 or 3 independently selected Rᶠ substituents; each Rᵉ is independently selected from H, D, CN, C₁₋₆ alkyl, C₁₋₄ haloalkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₆₋₁₀ aryl, C₃₋₁₀ cycloalkyl, 5-10 membered heteroaryl, heterocycloalkyl 4-10 membered, C₆₋₁₀-C₁₋₄-alkyl, C₃₋₁₀-C₁₋₄-cycloalkyl, (5-10 membered heteroaryl) -C₁₋₄- alkyl and (4-10 membered heterocycloalkyl) ) -C₁₋₄ alkyl-, where each of the C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₆₋₁₀ aryl, C₃₋₁₀ cycloalkyl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl , C₆₋₁₀-C₁₋₄-alkyl-, C₃₋₁₀-cycloalkyl-C₁₋₄- alkyl, (5-10 membered heteroaryl) -C₁₋₄- alkyl and (4-10 membered heterocycloalkyl) -C₁₋ alkyl ₄- of Rᵉ is optionally substituted with 1, 2 or 3 independently selected Rᵍ substituents; each Rᵍ is independently selected from H, D, C₁₋₆ alkyl, C₁₋₄ haloalkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₆₋₁₀ aryl, C₃₋₁₀ cycloalkyl, 5-10 membered heteroaryl, 4-heterocycloalkyl - 10 members, C₆₋₁₀-aryl-C alquilo-alkyl, C₃₋₁₀-cycloalkyl-C₁₋₄-alkyl, (5-10-membered heteroaryl) -C₁₋₄ -alkyl and (4-10-membered heterocycloalkyl) - C₁₋₄- alkyl, where each of the C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₆₋₁₀ aryl, C₃₋₁₀ cycloalkyl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, aryl C₆₋₁₀-C₁₋₄-alkyl, C₃₋₁₀-cycloalkyl-C₁₋₄-alkyl, (5-10 membered heteroaryl) -C₁₋₄-alkyl and (4-10-membered heterocycloalkyl) -C₁₋₄-alkyl of Rᵍ is optionally substituted with 1, 2 or 3 independently selected Rᵖ substituents; each Rᵖ is independently selected from C₁₋₄ alkyl, C₁₋₄ haloalkyl C₂₋₆, C₂₋₆ alkynyl C₂₋₆ aryl, C₃₋₁₀ cycloalkyl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, C₆ aryl ₋₁₀-C₁₋₄-alkyl, C₃₋₁₀-cycloalkyl-C₁₋₄-alkyl, (5-10 membered heteroaryl) -C₁₋₄-alkyl and (4-10-membered heterocycloalkyl) -C₁₋₄-alkyl alkyl, halo, CN, NHORʳ, ORʳ, SRʳ, C (O) Rʳ, C (O) NRʳRʳ, C (O) ORʳ, OC (O) Rʳ, OC (O) NRʳRʳ, NHRʳ, NRʳRʳ, NRʳC (O) Rʳ, NRʳC (O) NRʳRʳ, NRʳC (O) ORʳ, C (= NRʳ) NRʳRʳ, NRʳC (= NRʳ) NRʳRʳ, NRʳC (= NOH) NRʳRʳ, NRʳC (= NCN) NRʳRʳ, SF₅, -P (O) RʳRʳ, P (O) (ORʳ) (ORʳ), S (O) Rʳ, S (O) NRʳRʳ, S (O) ₂Rʳ, NRʳS (O) ₂Rʳ, NRʳS (O) ₂NRʳRʳ and S (O) ₂NRʳRʳ; or any two Rᵃ¹ substituents together with the nitrogen atom to which they are coupled form a 4, 5, 6, 7, 8, 9 or 10-membered heterocycloalkyl group, optionally substituted with 1, 2 or 3 independently selected R sustitu substituents; each Rʰ is independently selected from C₁₋₆ alkyl, C₃₋₁₀ cycloalkyl, 4-7 membered heterocycloalkyl, C₆₋₁₀ aryl, 5-6 membered heteroaryl, C₃₋₁₀ cycloalkyl-C₁₋₄- alkyl, (5-heteroaryl - 6 members) -C₁₋₄ alkyl-, (4-7 membered heteroaryl) -C₁₋₄ alkyl-, C₁₋₆ haloalkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, halo, CN, ORⁱ, SRⁱ, NHORⁱ C (O) Rⁱ, C (O) NRⁱRⁱ, C (O) ORⁱ, OC (O) Rⁱ, OC (O) NRⁱRⁱ, NHRⁱ, NRⁱRⁱ, NRⁱC (O) Rⁱ, NRⁱC (O) NRⁱRⁱ, NRⁱC (O) ORⁱ, C (= NRⁱ) NRⁱRⁱ, NRⁱC (= NRⁱ) NRⁱRⁱ, NRⁱC (= NOH) NRⁱRⁱ, NRⁱC (= NCN) NRⁱRⁱ, SF₅, -P (O) RⁱRⁱ, -P (O) (ORⁱ) (ORⁱ) , S (O) Rⁱ, S (O) NRⁱRⁱ, S (O) ₂Rⁱ, NRⁱS (O) ₂Rⁱ, NRⁱS (O) ₂NRⁱRⁱ and S (O) ₂NRⁱRⁱ, where each of the alkyl C₁₋₆, cycloalkyl C₃₋₁₀ , 4-7 membered heterocycloalkyl, C₆₋₁₀ aryl, 5-6 membered heteroaryl, C₃₋₁₀ cycloalkyl-C₁ alkyl ₄-, (5-6 membered heteroaryl) -C₁₋₄ alkyl-, (4-7 membered heterocycloalkyl) -C₁₋₄ alkyl of Rʰ is optionally further substituted with 1, 2 or 3 independently selected Rʲ substituents ; each Rʲ is independently selected from C₃₋₆ cycloalkyl, C₆₋₁₀ aryl, 5- or 6-membered heteroaryl, C₂₋₄ alkenyl, C₂₋₄ alkynyl, halo, C₁₋₄ alkyl, C₁₋₄ haloalkyl, CN, NHORᵏ, ORᵏ , SRᵏ, C (O) Rᵏ, C (O) NRᵏRᵏ, C (O) ORᵏ, OC (O) Rᵏ, OC (O) NRᵏRᵏ, NHRᵏ, NRᵏRᵏ, NRᵏC (O) Rᵏ, NRᵏC (O) NRᵏRᵏ, NRᵏC (O) ORᵏ, C (= NRᵏ) NRᵏRᵏ, NRᵏC (= NRᵏ) NRᵏRᵏ, NRᵏC (= NOH) NRᵏRᵏ, NRᵏC (= NCN) NRᵏRᵏ, SF₅, -P (O) RᵏRᵏ, -P (O) (ORᵏ) (ORᵏ), S (O) Rᵏ, S (O) NRᵏRᵏ, S (O) ₂Rᵏ, NRᵏS (O) ₂Rᵏ, NRᵏS (O) ₂NRᵏRᵏ and S (O) ₂NRᵏRᵏ; or two Rʰ groups coupled to the same carbon atom of the 4-10 membered heterocycloalkyl taken together with the carbon atom to which they are coupled form a C₃₋₆ cycloalkyl or a 4-6 membered heterocycloalkyl having 1-2 heteroatoms as members from the ring selected from O, N or S; or any two Rᵃ² substituents together with the nitrogen atom to which they are coupled form a 4, 5, 6, 7, 8, 9 or 10-membered heterocycloalkyl group, optionally substituted with 1, 2 or 3 Rʰ substituents; or any two Rᶜ substituents, together with the nitrogen atom to which they are coupled, form a heterocycloalkyl group of; 4, 5, 6 or 7 members optionally substituted with 1, 2 or 3 independently selected Rʰ substituents; or any two Rᵉ substituents, together with the nitrogen atom to which they are coupled, form a 4, 5, 6 or 7-membered heterocycloalkyl group optionally substituted with 1, 2 or 3 independently selected Rʰ substituents; or any two Rᵍ substituents, together with the nitrogen atom to which they are coupled, form a 4, 5, 6 or 7-membered heterocycloalkyl group optionally substituted with 1, 2 or 3 independently selected Rʰ substituents; or any two Rⁱ substituents, together with the nitrogen atom to which they are coupled, form a 4, 5, 6 or 7-membered heterocycloalkyl group optionally substituted with 1, 2 or 3 independently selected Rʰ substituents; or any two Rᵏ substituents, together with the nitrogen atom to which they are coupled, form a 4, 5, 6 or 7-membered heterocycloalkyl group optionally substituted with 1, 2 or 3 independently selected Rʰ substituents; or any two Rᵒ substituents, together with the nitrogen atom to which they are coupled, form a heterocycloalkyl group of 4, 5, 6 or 7, members optionally substituted with 1, 2 or 3 independently selected Rʰ substituents; or any two Rʳ substituents, together with the nitrogen atom to which they are coupled, form a 4, 5, 6 or 7-membered heterocycloalkyl group optionally substituted with 1, 2 or 3 independently selected Rʰ substituents; each Rⁱ, Rᵏ, Rᵒ or Rʳ is independently selected from H, D, C₁₋₄ alkyl, C₃₋₆ cycloalkyl, C₆₋₁₀ aryl, 5 or 6 membered heteroaryl, C₁₋₄ haloalkyl, C₂₋₄ alkenyl and C₂ alkynyl ₋₄, where each of the C₁₋₄ alkyl, C₃₋₆ cycloalkyl, C₆₋₁₀ aryl, 5- or 6-membered heteroaryl, C₂₋₄ alkenyl and C₂₋₄ alkynyl of Rⁱ, Rᵏ, Rᵒ or Rʳ is optionally substituted with 1, 2 or 3 independently selected Rq substituents; each Rq is independently selected from D, OH, CN, -COOH, NH₂, halo, C₁₋₆ alkyl, C₁₋₆ haloalkyl, C₁₋₆ alkoxy, C₁₋₆ haloalkoxy, C₁₋₄ alkylthio, phenyl, 5 - heteroaryl 6 members, C₃₋₆ cycloalkyl, 4-6 membered heterocycloalkyl, -CONHR¹², -NHC (O) R¹², -OC (O) R¹², -C (O) OR¹², -C (O) R¹², -SO₂R¹², - NHSO₂R¹², -SO₂NHR¹² and NR¹²R¹², where each of the C₁₋₆ alkyl, phenyl, 4-6 membered heterocycloalkyl and 5-6 membered heteroaryl of Rq is optionally substituted with OH, CN, -COOH, NH₂, C₁₋₆ alkoxy , C₃₋₆ cycloalkyl or 4-6 membered heterocycloalkyl; and each R¹² is independently C₁₋₆ alkyl; provided that: when R⁷ is C₁₋₆ alkyl, R¹⁰-L- is not cyclopropylsulfamoyl and methanesulfonamido; when R⁷ is cyclopropylmethyl, R¹⁰-L- is not methanesulfonamido; when R⁷ is 2- (4-morpholino) ethyl, R¹⁰-L- is not methanesulfonyl; and the compound is not 3- (8-aminoimidazol1,2-a] pyridin-3-yl) -2- (1H-tetrazol-5-yl) benzenesulfonamide. |
| priorityDate | 2016-06-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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Total number of triples: 40.